IKMC
IKMC provides comprehensive access to knockout mouse resources to systematically mutate and study all protein-coding genes in the mouse genome for gene function and human disease research.
Key Features:
- Systematic mutagenesis: Uses gene targeting and gene trapping in mouse embryonic stem (ES) cells to generate mutations in protein-coding genes.
- Resource records: Stores detailed information on knockout vectors, ES cells, and mice corresponding to specific genes.
- Central hub: Maintains a centralized database and web portal at www.knockoutmouse.org for consortium coordination and prioritization.
- Community integration: Integrates IKMC data with other community databases to facilitate data interconnections.
- BioMart integration: Employs the BioMart data management system to provide integrated access and to incorporate gene annotation, expression, phenotype, and disease-related data from external BioMarts.
Scientific Applications:
- Gene function analysis: Enables systematic loss-of-function studies across the mouse genome to elucidate gene roles.
- Genetic basis of human disease: Facilitates selection and use of knockout vectors, ES cells, and mice to study disease-relevant genes and phenotypes.
Methodology:
Data integration via the BioMart data management system to combine IKMC datasets with external BioMarts containing gene annotation, expression, phenotype, and disease-related data, together with database-driven coordination and prioritization.
Topics
Details
- Tool Type:
- web application
- Operating Systems:
- Linux, Windows, Mac
- Programming Languages:
- Java, Python
- Added:
- 3/27/2017
- Last Updated:
- 12/10/2018
Operations
Data Inputs & Outputs
Deposition
Publications
Ringwald M, et al. The IKMC web portal: a central point of entry to data and resources from the International Knockout Mouse Consortium. Nucleic Acids Res. 2011; 39:D849-55. doi: 10.1093/nar/gkq879
Oakley DJ, et al. BioMart as an integration solution for the International Knockout Mouse Consortium. Database (Oxford). 2011; 2011:bar028. doi: 10.1093/database/bar028